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Jeanette Erdmann is Deputy Editor at Circulation: Genomic and Precision Medicine.
Effective January 2020, Jeanette Erdmann is Deputy Editor at Circulation: Genomic and Precision Medicine. https://www.ahajournals.org/journal/circgen
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Guest lecture by Valerie Allamand about Collagen VI-deficiency and its consequences on the myomatrix
On November 27, 2019 at 3 pm in the seminar room EG (MFC1) the guest lecture given by Valerie Allamand will take place. You are ...
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Ambassador for Muscle Disease Patients
In today’s issue of Lübecker Nachrichten, our local daily newspaper, an article was published about our work on collagen-6 myopathy.
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Deutsche Gesellschaft für Muskelkranke e.V (DGM)
Raising awareness for rare diseases is extremely important. As a patient affected with a rare disease (Collagen 6 congenital muscular dystrophy) Jeanette Erdmann, director of ...
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Research Topic: From GWAS hits to treatment targets – published as an eBook
The Research Topic: “From GWAS hits to treatment targets” was accompanied by a symposium held in Lübeck on January 12th, 2018. The agenda and pics ...
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Jeanette Erdmann joined Circulation: Genomic and Precision Medicine as Senior Guest Editor
Effective Mid August 2019 until End of July 2021, Jeanette Erdmann joined the team of Circulation: Genomic and Precision Medicine as Senior Guest Editor. The ...
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PlaqOmics progress meeting in Lübeck
On Sunday April 7th we will welcome our colleagues and collaborators from the PlaqOmics consortium for a two-days progress meeting. PlaqOmics is funded by the ...
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Den genetischen Ursachen angeborener Herzfehler auf der Spur
Mithilfe modernster Genanalysemethoden konnte ein deutsches Forscherteam zeigen, dass ein komplexer angeborener Herzfehler seinen Ursprung in mehreren Genen hat und wie diese Genveränderungen zusammenwirken. Das ...
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First joint BHF/DZHK consortium gets funding
Great news for our institute and the whole consortium! We succeeded to get funded jointly by the BHF and DZHK (2.4 Mio € in total ...
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Wir machen mit!
Fast schon eine Tradition, auch in diesem Jahr nimmt das ICG am “Girl´s Day” 2019 teil! In diesem Jahr findet der “Girl´s Day” am 28.3.2019 ...
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The ICG is part of the gnomAD consortium
Over the next couple of months several papers co-authored by the gnomAD PIs, the Genome Aggregation Database Production Team and the Genome Aggregation Database Consortium ...
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A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A
This project is a prime example of perseverance. Finally, after 20 years of work we were able to unravel the multigenic origin of a congenital ...
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